A curated catalogue of human genomic structural variation

Variant Details

Variant: esv3892663

Internal ID

18836797

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr15:34450638..34496365	hg38	UCSC Ensembl
Outer	chr15:34426393..34515668	hg38	UCSC Ensembl
Inner	chr15:34742839..34788566	hg19	UCSC Ensembl
Outer	chr15:34718594..34807869	hg19	UCSC Ensembl
Inner	chr15:32530131..32575858	hg18	UCSC Ensembl
Outer	chr15:32505886..32595161	hg18	UCSC Ensembl

Cytoband

15q14

Allele length

Assembly	Allele length
hg38	89276
hg19	89276
hg18	89276

Variant Type

CNV gain+loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

essv25789365, essv25785175, essv25800694, essv25797986, essv25797909, essv25801241, essv25800533, essv25779632, essv25786042, essv25796442, essv25792505, essv25796111, essv25797913, essv25779950, essv25798315, essv25798075, essv25792618, essv25780343, essv25796650, essv25796294, essv25796652, essv25796675, essv25779118, essv25798055, essv25794459, essv25781558, essv25782975, essv25784344, essv25786182, essv25794782, essv25798050, essv25779231, essv25793425, essv25798854, essv25787681, essv25797147, essv25801500, essv25786179, essv25778505, essv25800489, essv25780382, essv25797398, essv25796032, essv25800762, essv25787427, essv25783418, essv25795015, essv25792961, essv25780529, essv25800347, essv25793158, essv25785393, essv25791577, essv25782405, essv25782274, essv25799913, essv25791023, essv25800527, essv25792678, essv25800575, essv25796541, essv25796632, essv25796425, essv25785103, essv25781274, essv25797417, essv25790997, essv25800267, essv25800068, essv25796431, essv25797783, essv25778293, essv25781016, essv25797581, essv25797708, essv25795994, essv25796153, essv25796410, essv25778414, essv25782636, essv25794866, essv25778444, essv25799956, essv25800887, essv25786238, essv25788222, essv25786194, essv25796564, essv25786687, essv25797301, essv25786429, essv25796769, essv25800405, essv25785317, essv25782347, essv25797138, essv25797629, essv25801021, essv25781704, essv25787937, essv25797098, essv25789403, essv25796236, essv25779032, essv25800163, essv25792659, essv25798062, essv25797625, essv25781638, essv25782457, essv25800472, essv25795333, essv25794974, essv25800210, essv25793343, essv25797090, essv25778429, essv25800943, essv25798698, essv25796055, essv25783739, essv25797043, essv25797024, essv25800552, essv25792648, essv25797129, essv25796192, essv25780090, essv25797376, essv25792810, essv25780229, essv25796941, essv25787881, essv25780509, essv25786890, essv25796707, essv25786361, essv25799380, essv25786038, essv25784679, essv25788769, essv25782664, essv25797530, essv25797903, essv25786562, essv25800922, essv25796176, essv25798238, essv25800831, essv25781059, essv25784446, essv25780818, essv25796268, essv25796080, essv25783833, essv25786156, essv25784721, essv25785920, essv25786383, essv25797595, essv25779621, essv25796116, essv25798443, essv25801402, essv25784753, essv25786574, essv25783300, essv25796525

Samples

Known Genes

Method

SNP array

Analysis

Platform

Illumina HumanHap 550
Illumina HumanHap 610
Illumina Human OmniExpress

Comments

Reference

Suktitipat_et_al_2014

Pubmed ID

Accession Number(s)

Frequency

Sample Size	3017
Observed Gain	15
Observed Loss	153
Observed Complex	0
Frequency	n/a